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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2387021생성일: 2026년 10월 25일

3-Ethylphenol → 4-Ethyl-2-hydroxybenzaldehyde

https://huagongshe.com/reaction/2387021

반응식

참여 물질

역할이름HCID투입량
반응물3-EthylphenolHCID 12101—
반응물Methane, dichloromethoxy-HCID 21004—
촉매Titanium TetrachlorideHCID 24193—
생성물4-Ethyl-2-hydroxybenzaldehydeHCID 1023601765.3%

반응 단계

Titanium(IV) chloride (100 mL, 100 mmol, 1M in CH2Cl2) followed by dichloromethyl methyl ether (7.47 mL, 82.5 mmol) was added to a cooled 0° C. solution of 3-ethylphenol (6.11 g, 50 mmol). The reaction mixture was stirred for 45 mins. The mixture was poured into ice and extracted with EtOAc. The organic layers were washed with brine, dried over Na2SO4 and concentrated to a bright pink oil. Purification by flash column chromatography (0% to 10% EtOAc in hexanes) gave 4-ethyl-2-hydroxy-benzaldehyde (4.9 g, 65%) followed by 2-ethyl-4-hydroxy-benzaldehyde (1.32 g, 18%). A: 1H NMR (400 MHz, CDCl3): δ 1.25 (t, J=7.6 Hz, 3 H), 2.67 (d, J=7.6 Hz, 2 H), 6.82 (s, 1 H), 6.85 (d, J=8.0 Hz, 1 H), 7.46 (t, J=8.0 Hz, 1 H), 9.83 (s, 1 H), 11.05 (s, 1 H). B: 1H NMR (400 MHz, CDCl3): δ 1.27 (t, J=7.6 Hz, 3 H), 3.03 (d, J=7.6 Hz, 2 H), 6.68 (s, 1 H), 6.78 (s, 1 H), 6.82 (d, J=8.3 Hz, 1 H), 7.77 (t, J=8.3 Hz, 1 H), 10.10 (s, 1 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08268835B2
출처 데이터셋uspto-grants-2012_09
ORD IDord-521b495bb2af4e898272e25ab57e6c39
출처 메모uspto-grants-2012_09